510(k) K142995 ยท MUH System, X-Ray, Extraoral Source, Digital
SOPIX
| Applicant | Sopro - Acteon Group, Laciotat, FR |
| Decision | Substantially Equivalent, Aug 17, 2015 |
| Received | Oct 16, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142995
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.